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Selection for Cell Yield Does Not Reduce Overflow Metabolism in Escherichia coli
Overflow metabolism is ubiquitous in nature, and it is often considered inefficient because it leads to a relatively low biomass yield per consumed carbon. This metabolic strategy has been described as advantageous because it supports high growth rates during nutrient competition. Here, we experimen...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789295/ https://www.ncbi.nlm.nih.gov/pubmed/34893866 http://dx.doi.org/10.1093/molbev/msab345 |
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author | Rabbers, Iraes Gottstein, Willi Feist, Adam M Teusink, Bas Bruggeman, Frank J Bachmann, Herwig |
author_facet | Rabbers, Iraes Gottstein, Willi Feist, Adam M Teusink, Bas Bruggeman, Frank J Bachmann, Herwig |
author_sort | Rabbers, Iraes |
collection | PubMed |
description | Overflow metabolism is ubiquitous in nature, and it is often considered inefficient because it leads to a relatively low biomass yield per consumed carbon. This metabolic strategy has been described as advantageous because it supports high growth rates during nutrient competition. Here, we experimentally evolved bacteria without nutrient competition by repeatedly growing and mixing millions of parallel batch cultures of Escherichia coli. Each culture originated from a water-in-oil emulsion droplet seeded with a single cell. Unexpectedly we found that overflow metabolism (acetate production) did not change. Instead, the numerical cell yield during the consumption of the accumulated acetate increased as a consequence of a reduction in cell size. Our experiments and a mathematical model show that fast growth and overflow metabolism, followed by the consumption of the overflow metabolite, can lead to a higher numerical cell yield and therefore a higher fitness compared with full respiration of the substrate. This provides an evolutionary scenario where overflow metabolism can be favorable even in the absence of nutrient competition. |
format | Online Article Text |
id | pubmed-8789295 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-87892952022-01-26 Selection for Cell Yield Does Not Reduce Overflow Metabolism in Escherichia coli Rabbers, Iraes Gottstein, Willi Feist, Adam M Teusink, Bas Bruggeman, Frank J Bachmann, Herwig Mol Biol Evol Discoveries Overflow metabolism is ubiquitous in nature, and it is often considered inefficient because it leads to a relatively low biomass yield per consumed carbon. This metabolic strategy has been described as advantageous because it supports high growth rates during nutrient competition. Here, we experimentally evolved bacteria without nutrient competition by repeatedly growing and mixing millions of parallel batch cultures of Escherichia coli. Each culture originated from a water-in-oil emulsion droplet seeded with a single cell. Unexpectedly we found that overflow metabolism (acetate production) did not change. Instead, the numerical cell yield during the consumption of the accumulated acetate increased as a consequence of a reduction in cell size. Our experiments and a mathematical model show that fast growth and overflow metabolism, followed by the consumption of the overflow metabolite, can lead to a higher numerical cell yield and therefore a higher fitness compared with full respiration of the substrate. This provides an evolutionary scenario where overflow metabolism can be favorable even in the absence of nutrient competition. Oxford University Press 2021-12-06 /pmc/articles/PMC8789295/ /pubmed/34893866 http://dx.doi.org/10.1093/molbev/msab345 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Discoveries Rabbers, Iraes Gottstein, Willi Feist, Adam M Teusink, Bas Bruggeman, Frank J Bachmann, Herwig Selection for Cell Yield Does Not Reduce Overflow Metabolism in Escherichia coli |
title | Selection for Cell Yield Does Not Reduce Overflow Metabolism in Escherichia coli |
title_full | Selection for Cell Yield Does Not Reduce Overflow Metabolism in Escherichia coli |
title_fullStr | Selection for Cell Yield Does Not Reduce Overflow Metabolism in Escherichia coli |
title_full_unstemmed | Selection for Cell Yield Does Not Reduce Overflow Metabolism in Escherichia coli |
title_short | Selection for Cell Yield Does Not Reduce Overflow Metabolism in Escherichia coli |
title_sort | selection for cell yield does not reduce overflow metabolism in escherichia coli |
topic | Discoveries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789295/ https://www.ncbi.nlm.nih.gov/pubmed/34893866 http://dx.doi.org/10.1093/molbev/msab345 |
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